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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3216Erstellt: 23. Oktober 2026

Acetic Acid → 2-aminopyrido[2,3-d]pyrimidin-7(8H)-one 55

https://huagongshe.com/de/reaction/3216

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktEthyl 3-aminobenzoateHCID 11400—
Edukt6-(2,6-Dichlorophenyl)-8-methyl-2-methylsulfonyl-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 10596157—
LösungsmittelWaterHCID 962—
Produkt2-aminopyrido[2,3-d]pyrimidin-7(8H)-one 55HCID 5327901—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 0.226 g (0.58 mmol) of 6-(2,6-dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 39 and 0.40 g (2.42 mmol) of 3-aminobenzoic acid, ethyl ester was fused in a 170° C. oil bath to give a clear melt. After 6 minutes, the melt was cooled to ca. 100° C. Glacial acetic acid (1 mL) was added to dissolve the melt. Water (5 mL) was added to precipitate a solid. The solid was filtered, washed well with water, and triturated with 2 mL of methanol. The mixture was filtered, and the cake was washed with 1 mL of methanol and then ether; wt 0.194 g. Recrystallization from ethyl acetate gave pure product; wt 0.075 g; mp 238°-240° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05733914
Quelldatensatzuspto-grants-1998_03
ORD IDord-9fd5cd2b22e5454fb149f6f3ed738293
Quellennotizuspto-grants-1998_03